Use of certain isoquinolinesulfonyl compounds for the treatment of glaucoma and ocular ischemia

ABSTRACT

Isoquinolinesulfonyl compounds are used in ophthalmic compositions to treat glaucoma or other ischemic-borne ocular disorders such as retinopathies or optic neuropathies. These compounds vasodilate ocular blood vessels, lower IOP and prevent or reduce the progression of visual field loss.

This application is a continuation in part of Ser. No. 09/077,575 filed on Jan. 9, 1999, now U.S. Pat. No. 6,271,224 which is a 371 of PCT/US96/20197 filed on Dec. 20, 1996.

This application claim benefit to provisional application No. 60/009,351 Dec. 21, 1995.

BACKGROUND OF THE INVENTION

The present invention relates generally to the field of ophthalmology. In particular, the invention relates to the treatment of ocular disorders including visual field loss and glaucoma using an isoquinolinesulfonyl compound, which lowers intraocular pressure (IOP) and produces dilation of ocular blood vessels.

Although the underlying causes of glaucoma are not fully understood at this time, glaucoma is characterized by damage to the optic nerve head, accompanied by a decrease in the normal visual field. One risk factor for glaucomatous visual field loss is elevated IOP. In fact, glaucoma has historically been treated by drug and/or surgical therapy to lower elevated IOP. While elevated IOP has been positively correlated with the rate of progression of visual field loss in glaucoma, visual field loss may occur at levels of IOP which are considered within the normal range. Thus, other factors, along or in addition to elevated IOP, may influence the occurrence and rate of progression of visual field loss.

To remain healthy and function normally, the retina and the optic nerve head fibers (neurons) must receive a proper supply of nutrients and oxygen, and must have their carbon dioxide and other metabolic waste products removed. This is accomplished by the microcirculation in these tissues. As used herein, the term “microcirculation” refers to the blood flow through the nutritive blood vessels, across whose walls nutrients, gases and waste products move. Blood flow to the eye depends upon the perfusion pressure (the systemic blood pressure minus the IOP). Some tissues have the ability to maintain (i.e., autoregulate) blood flow through a range of perfusion pressures such that an increase in systemic blood pressure may cause a reduction in the caliber of the blood vessel lumen. Conversely, reduction in systemic pressure in such tissues can result in vessel dilation; however, there is a point where perfusion pressure falls to such a level that the vessel is maximally dilated. Any further fall in perfusion pressure results in a reduction of blood flow to the tissue (ischemia). Ischemia may also result from obstruction, vasospasm, increased vascular resistance, or other interference with microcirculation. Prolonged ischemia ultimately can result in tissue necrosis or neuronal cellular apoptosis. In the case of the optic nerve head or retina, a state of visual dysfunction may precede the death of the neurons. Hence, if ischemia is involved in the death of optic nerve fibers due to glaucoma or some other ischemic-borne retinopathies or optic neuropathies, then its prevention could protect the neurons from death or loss of function.

The vasodilatory and spasmolytic activities of certain isoquinolinesulfonyl compounds have been described with respect to non-ocular tissues. See, e.g., EP 0 187 371 B1, which corresponds to U.S. Pat. No. 4,678,783. These vascular attributes are likely associated with inhibition of myosin-light chain kinase activity. Myosin-light chain kinase is an enzyme necessary for the excitation-contraction coupling of contractile activity in vascular smooth muscle. Inhibition of this enzyme results in vascular smooth muscle relaxation (i.e., vasodilation) which can product an increased blood flow.

SUMMARY OF THE INVENTION

The inventors believe that microcirculatory disturbances that restrict nutritive blood flow to the choroid, retina and optic nerve head are likely involved in the progression of visual field loss. While bound by no theories, the inventors postulate that compounds which enhance oxygen and nutrient delivery by enhancing ocular blood flow may be beneficial in preventing optic nerve head injury and may subsequently prevent or alter the rate of progression of visual field loss associated with glaucoma and ischemic optic neuropathies.

The present invention provided compositions and methods useful in the treatment of glaucoma (with or without ocular hypertension) and ocular ischemia, which may result in retinopathies and optic neuropathies. The compositions contain an isoquinolinesulfonyl compound which is effective in reducing or preventing optic nerve head or retinal damage as well as reducing IOP in man or other mammals toward normal levels and thus, in reducing or preventing visual field loss.

In an alternative embodiment of the compositions and methods of the present invention, the above compositions may further include a mucomimetic polymer, a gelling polysaccharide, a finely divided drug carrier substrate (defined below), or a combination of these components. These additional components provide compositions which enhance comfort and provide sustained release and delivery of the drug to the eye.

DETAILED DESCRIPTION OF THE INVENTION

Elevation of IOP is associated with clinical manifestations characteristic of glaucomatous optic neuropathy. Optic nerve dysfunction may be the result of pressure-induced changes in the structure of the optic nerve head and/or reduced circulation to the optic nerve head and retina. In addition to affecting vascular resistance and blood flow, the inventors have discovered that certain isoquinolinesulfonyl compounds also lower intraocular pressure.

The isoquinolinesulfonyl compounds of the present invention are the compounds of formula (I) shown below, as well as their pharmaceutically acceptable salts.

wherein R¹ represents a hydrogen atom, a chlorine atom or a hydroxyl group; and when R¹ represents a hydrogen atom,

A represents an ethylene group unsubstituted or substituted with an alkyl group having 1 to 6 carbon atoms, a phenyl group or a benzyl group,

R² and R³ are directly bonded with each other, thereby forming a trimethylene group unsubstituted or substituted with an alkyl group having 1 to 6 carbon atoms, a phenyl group or a benzyl group, and

R⁴ represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms; and

when R¹ represents a chlorine atom or a hydroxyl group,

A represents an alkylene group having 2 to 6 carbon atoms, said group being unsubstituted or substituted with an alkyl group having 1 to 6 carbon atoms,

R² and R³ are not bonded with each other and each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, or R² and R³ are directly bonded with each other, thereby forming an ethylene group unsubstituted or substituted with an alkyl group having 1 to 6 carbon atoms or a trimethylene group unsubstituted or substituted with alkyl group having 1 to 6 carbon atoms, and

R⁴ represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an amidino group;

and pharmaceutically acceptable salts thereof.

Some preferred compounds of the invention are represented by the following formula (IA):

wherein:

R¹=H, OH, or Cl;

A=an ethylene group, unsubstituted or substituted with an alkyl group having 1 to 6 carbons;

R⁴=H or an alkyl group having 1 to 3 carbons;

R⁵—an alkyl group having 1 to 3 carbons; and

R⁶=H or an alkyl group having 1 to 6 carbons; together with pharmaceutically acceptable salts thereof; with the proviso that the following compounds are excluded:

 and pharmaceutically acceptable salts thereof.

The above-mentioned alkyl groups may be a straight chain or a branched chain group. These compounds and methods of their syntheses are disclosed in U.S. Pat. No. 4,678,783, the entire contents of which are incorporated herein by this reference. Other isoquinolinesulfonyl derivatives and methods of their syntheses are disclosed in U.S. Pat. No. 4,525,589, the entire contents of which are likewise incorporated herein by this reference.

Preferred compounds of the formula (IA) are those wherein:

R⁴=H, OH, or Cl;

A—an ethylene group unsubstituted or substituted with an alkyl group having 1 to 3 carbons;

R⁴=H or an alkyl group having 1 to 3 carbon;

R⁵=an alkyl group having 1 to 3 carbons; and

R⁶=H or an alkyl group having 1 to 6 carbons.

Most preferred compounds of the formula (IA) are those wherein:

R¹=H, OH, or Cl;

A=an ethylene group unsubstituted or substituted with an alkyl group having 1 to 3 carbons;

R⁴=H;

R⁵=an alkyl group having 1 carbon; and

R⁶=H or an alkyl group having 1 to 3 carbons.

Particularly preferred among the foregoing compounds is 1-(5-isoquinolinesulfonyl)-2,5-dimethylpiperazine exemplified below, which has the structure of formula (IA) wherein:

R¹, R⁴ and R⁶=H; and

A=an ethylene group substituted with an alkyl group having 1 carbon.

The preferred isoquinolinesulfonyl compound of formula I the present invention is hexahydro-1-(5-isoquinolinylsulfonyl)-1H-1,4-diazepine, also known as 1-(5-soquinolinesulfonyl)-homopiperazine, and shown below as Compound (II), as well as its pharmaceutically acceptable salts.

Most preferred among the compounds of formula (I) is the hydrochloride salt of Compound (II). The hydrochloride salt of Compound (II), known as fasudil, AT-877, and HA-1077 is manufactured by Asahi Chemical Industry Co., Ltd. (Japan).

Alternatively, Compound (II) and a preferred metabolite thereof may be represented by the following formula:

wherein R=H or OH.

In general, for topical administration an amount of an isoquinolinesulfonyl compound between about 0.001 and about 10.0 percent by weight (wt %) is used in the compositions of the present invention. It is preferred that between about 0.01 and about 3.0 wt % is used, and it is especially preferred to use an amount between about 0.1 and about 2.0 wt %.

The compositions of the present invention may additionally include components to provide sustained release and/or comfort. Such components include mucomimetic polymers, gelling polysaccharides and finely-divided drug carrier substrates. These components are discussed in greater detail in U.S. Pat. No. 4,911,920 issued Mar. 27, 1990 and in U.S. Pat. No. 5,212,162 issued May 18, 1993. The entire contents of these two patents are incorporated herein by reference. For purposes of this invention, the term “mucomimetic polymers” includes carbomers (discussed below), mucopolysaccharides (e.g. hyaluronic acid and chondroitin sulfate) and cellulosic polymers (e.g., methyl cellulose, hydroxy propyl methyl cellulose, hydroxyethyl cellulose, carboxy methyl cellulose, and hydroxy propyl cellulose).

The preferred mucomimetic polymers useful in the present invention are anionic and have a molecular weight between about 50,000 and 6 million daltons. These preferred polymers are characterized as having carboxylic acid functional groups and preferably contain between 2 and 7 carbon atoms per functional group. The gels which form during preparation of the ophthalmic polymer dispersion have a viscosity between about 1,000 to about 300,000 centipoise (cps). Suitable polymers are carboxy vinyl polymers, preferably those called carbomers, e.g., CARBOPOL® (Goodrich Co., Cleveland, Ohio). Specifically preferred are CARBOPOL® 934 and 940. Such polymers will typically be employed in an amount between about 0.05 and about 8.0 wt %, depending on the desired viscosity of the composition. Pourable liquid compositions generally comprise an amount of the polymer between about 0.05 and about 2.0 wt %.

As used herein, the term “finely-divided drug carrier substrate” (or “DCS”) means finely-divided solids, colloidal particles, or soluble polymers and/or polyelectrolytes which are capable of selective adsorption or binding with drug molecules. Examples of DCS include, but are not limited to: finely divided silica, such as fumed silica, silicates and bentonites; ion exchange resins, which can be anionic, cationic or non-ionic in nature; and soluble polymers, such as, alginic acid, pectin, soluble carrageenans, CARBOPOL®, and polystyrene sulfonic acid. In general, the DCS component is used at a level in the range of about 0.05 to about 10.0 wt %. For particulate DCS, the average particle size diameter ranges from about 1 to about 20 microns. The amount of DCS and its characteristics (e.g., amount of cross-linking, particle size) may be varied in order to produce the desired time-release profile for the chosen drug.

Preferred DCS are the ion exchange resins. Some resins which are used in chromatography make ideal DCS for binding drugs in the compositions of the present invention. Such resins are readily available, for example, from Rohm & Haas (Philadelphia, Pa.) under the name AMBERLITE® and from Dow Chemical Co. (Midland, Mich.) under the name DOWEX®. The average particle size diameter of the commercially available forms of the resin is about 40 to about 150 microns. Such commercially available particles are most conveniently reduced to a particle size range of about 1.0 to about 25 microns by ball milling, according to known techniques. At least 95% of the resulting spherodial particles will preferably have a diameter less than 20 microns. The ion exchange resins will typically be present in an amount between about 0.05 and about 10.0 wt % and will have an average particle size diameter between about 1 and about 20 microns.

In addition to the above-described principal ingredients, the compositions of the present invention may further comprise various formulatory ingredients, such as antimicrobial preservatives and tonicity agents. Examples of suitable antimicrobial preservatives include: benzalkonium chloride, thimerosal, chlorobutanol, methyl paraben, propyl paraben, phenylethyl alcohol, edetate disodium, sorbic acid, polyquatemium 1 and other agents equally well-known to those skilled in the art. Such preservatives, if utilized, will typically be employed in am amount between about 0.001 and about 1.0 wt %. Examples of suitable agents which may be utilized to adjust the tonicity or osmolality of the formulations include: sodium chloride, potassium chloride, mannitol, dextrose, glycerin and propylene glycol. Such agents, if utilized, will typically be employed in an amount between about 0.1 and about 10.0 wt %.

As will be appreciated by those skilled in the art, the compositions may be formulated in various dosage forms suitable for topical ophthalmic delivery, including solutions, suspensions, emulsions, gels and erodible solid ocular inserts. The compositions are preferably aqueous, have a pH between about 3.5 and about 8.0 and an osmolality between about 280 and about 320 millOsmoles per kilogram (mOsm/kg).

The compositions of the present invention may also comprise non-aqueous formulations such as: substantially non-aqueous liquids, substantially non-aqueous semi-solid compositions, and solid compositions or devices. The first class, substantially non-aqueous liquids, includes a isoquinolinesulfonyl compound dissolved or suspended in one or more of the following: vegetable and mineral oils, such a liquid petrolatum, corn oil, castor oil, sesame oil, and peanut oil; triglycerides, such as the capric/caprylic triglycerides commonly used in foods and cosmetics; liquid lanolin and lanolin derivatives, and perfluorohydrocarbons. The second class, semi-solid compositions, comprises an isoquinolinesulfonyl compound dissolved or suspended in one or more of the following: various types of petrolatum, such as white, yellow, red and so on; lanolin and lanolin derivatives; gelled mineral oil having a hydrocarbon base, such as PLASTIBASE®; petrolatum and ethylene carbonate mixtures; petrolatum in combination with surfactants and polyglycol, such as polyoxyl 40 stearate and polyethylene glycol.

The third class, solid compositions or devices, includes an isoquinolinesulfonyl compound in association with (i) non-erodible devices which are inserted into the conjunctival sac of the eye and later removed, such as the Alza-type diffusion or osmotic pressure controlled polymer membranes, and (ii) bioerodible polymers which do not have to be removed from the conjunctival sac, such as essentially anhydrous but water soluble polymers and resins (e.g., celluloses, polycarboxylic acids, and so on). Especially preferred are the bioerodile inserts described and detailed in U.S. Pat. No. 4,540,408 (Lloyd) and U.S. Pat. No. 4,730,013 (Bondi et al.), wherein isoquinolinesulfonyl compounds of the present invention would be entrained in a non-aqueous matrix consisting essentially of polyvinyl alcohol. The entire contents of these two patents are incorporated herein by reference.

As will further be appreciated by those skilled in the art, the isoquinolinesulfonyl compounds of the present invention may also be administered intraocularly, periocularly or systemically (e.g. parenterally or orally).

Intraocular or periocular administration may be effected by incorporating a isoquinolinesulfonyl compound in a surgical irrigating solution used in ophthalmic surgery, or, preferably, by intravitreal or periocular injection. Such injection therapy will typically require from about 0.1 nM to about 1 mN (approximately 0.02 ng to 500 μg) of a isoquinolinesulfonyl compound for each eye treated. It is preferred that between about 200 nM and about 160 μM (approximately 40 ng to 80 μg) per eye be used in such therapy.

The preferred routes of systemic administration are oral and intravenous. Oral dosing of an isoquinolinesulfonyl compound in accordance with this invention will typically range from about 1.0 to about 1000 mg, one to four times per day. The preferred dosing range of oral administration is from about 10 to about 250 mg two to three times per day. Intravenous dosing of an isoquinolinesulfonyl compound in accordance with this invention will typically range from about 0.01 to about 100 mg, one to four times per day. The preferred dosing range for intravenous administration is from about 1.0 to about 30 mg, two to three times per day.

The present invention is also directed to methods of treating glaucoma and other ophthalmic diseases and abnormalities associated with visual field loss. The treatment may be effected by administering a therapeutically effective amount of an isoquinolinesulfonyl compound topically, intraocularly, periocularly or systemically. The preferred methods comprise topically applying to the affected eye(s) of the patient a therapeutically effective amount of a composition according to the present invention. The frequency and amount of dosage will be determined by the clinician based on various clinical factors. The preferred methods will typically comprise topical application of one or two drops of a 0.1% to 3.0% liquid formulation (or an equivalent amount of a solid or semi-solid dosage form) to the affected eye as needed, preferably one to four times per day. Topical ocular administration of a 0.2 to 2.0% liquid formulation is most preferred.

The following examples are presented to further illustrate various aspects of the present invention, but are not intended to limit the scope of the invention in any respect.

EXAMPLE A

The compounds of this invention may be prepared by the methods described in U.S. Pat. No. 4,678,783 and detailed in Scheme 1. 5-isoquinolinesulfonic acid (II, X═H) and 1-chloro-5-isoquinolinesulfonic acid (II, X═Cl) are known compounds that can be converted to the sulfonyl chloride (III) by treatment with thionyl chloride in the presence of dimethylformamide or by reaction with phosphorous pentachloride. Reaction with of isoquinolinesulfonyl chloride (III) with amine (IV) in a solvent such as methylene chloride, tetrahydrofuran, dioxane, N,N-dimethylformamide, acetonitrile or water in the presence of an acid acceptor provides compounds of formula V. Acid acceptors such as sodium bicarbonate, sodium carbonate or a tertiary amine such as pyridine or triethylamine may be used. An excess of the compound of formula IV (2 to 5 equivalents of the compound of formula IV per equivalent of compound of formula III) can also be used as the acid acceptor. The reaction of compounds of the formula III and compounds of the formula IV can be carried out at temperatures from −20° C. to 50° C. Typical reaction times are 0.5 to 24 hours.

The 1-chloro-5-isoquinolinesulfonamides of formula V(X═Cl) can be hydrolyzed to the corresponding 1-hydroxy-5-isoquinolinesulfonamides of formula VI by treatment with a 0.2 to 10 M solution of an inorganic acid such as hydrochloric, sulfuric or nitric acid at a temperature of 20° C. to 100° C. for 2 to 6 hours. Certain protecting groups and protecting and deprotecting steps may be used as would be apparent to one skilled in the art.

Compounds of formula (I) may exist as mixtures of stereoisomers. The preparation of individual stereoisomers may be effected by resolving the amines of formula (I) or by using other techniques known to those skilled in the art.

The amines of formula (I) may be converted to amine salts by reacting the amine with acids of sufficiently low pH to produce an amine salt. Pharmaceutically acceptable anions include: acetate, bromide, chloride, citrate, maleate, fumarate, mesylate, phosphate, sulfate and tartrate.

EXAMPLE B 1-(1-Chloro-5-isoguinolinesulfonyl)-3-methylpiperazine

To 40 mL of thionyl chloride is added 2.93 g of 1-chloro-5-isoquinolinesulfonic acid and 0.5 mL of N,N-dimethylformamide. The resulting mixture is warmed at 80° C. The volitiles are removed under reduced pressure to produce a residue. The residue is lo dissolved in water and the pH is adjusted to 6.0 with an aqueous sodium bicarbonate solution. The resulting mixture is extracted with methylene chloride and the resulting methylene chloride solution is combined with a solution of 2.8 g of 1-benzyloxycarbonyl 3-methyl piperazine and 1.8 of triethylamine in methylene chloride while the temperature is maintained at 0° C. After 1 hour the mixture is allowed to warm to ambient temperature and is stirred. The reaction mixture is washed with dilute hydrochloric acid, dried (anhydrous sodium sulfate) and concentrated. The residue is dissolved in methanol and 0.25 g of 5% palladium on charcoal is added to the solution. The reaction mixture is stirred at ambient temperature under a hydrogen atmosphere (40 psi). After the hydrogenolysis is complete, the reaction mixture is filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography to provide 1-(1-chloro-5-isoquinolinesulfonyl)-3-methylpiperazine.

EXAMPLE C 1-(1-Hydroxy-5-isoguinolinesulfonyl)-3-methylpiperazine

A mixture of 2.0 g 1-(1-chloro-5-isoquinolinesulfonyl)-3-methylpiperazine in 6 N hydrochloric acid was warmed at 70-80° C. The solid that forms is collected by filtration and is washed with water and ethanol to provide 1-(1-hydroxy-5-isoquinolinesulfonyl)-3-methylpiperazine.

EXAMPLE D 1-(5-Isoguinolinesulfonyl)-2.5-dimethylpinerazine

To 40 mL of thionyl chloride is added 2,50 g of 5-isoquinolinesulfonic acid and 0.5 mL of N,N-dimethylformamide. The resulting mixture is warmed at 80° C. The volitiles are removed under reduced pressure to produce a residue. The residue is dissolved in water and the pH is adjusted to 6.0 with an aqueous sodium bicarbonate solution and the resulting mixture is extracted with methylene chloride. The methylene chloride solution is combined with a solution of 2.8 g of 1-benzyloxycarbonyl-2,5-dimethylpiperazine and 1.8 of triethylamine in methylene chloride while the mixture is maintained at 0° C. After 1 hour, the reaction mixture is allowed to warm to ambient temperature and is stirred. The reaction mixture is washed with dilute hydrochloric acid, dried (anhydrous sodium sulfate) and concentrated under reduced pressure. The residue is dissolved in methanol and 0.25 g of 5% palladium on charcoal is added. The reaction mixture is stirred at ambient temperature under a hydrogen atmosphere (40 psi). After the hydrogenolysis is complete, the reaction mixture is filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography to provide 1-(5-isoquinolinesulfonyl)-2,5-dimethylpiperazine:

EXAMPLE E

Guinea Pig Hyper- emia (Cumu- lative MIOP IOP Com- over % Reduction pound 4 hours) Dose 1 3 6 Fasudil hexahydro-1-(5- 75  500 μg 21.9 14.6 23.4 isoquinolinyl- sulfonyl)-1H- 1,4-diazepine H-7 1-(5-isoquinoline- sulfonyl)- 0 1000 μg 30.9 20.9 11.6 3-methylpiperazine Example 1-(5-isoquinoline- D sulfonyl)- 20  500 μg 36.3 32.8 19.3 2,5-dimethylpipera- zine 1-(1-chloro-5- 10  500 μg 7.9 11.9 9.4 isoquinolinesul- fonyl)-piperazine

A guinea pig model was used to assess the potential of the compounds to cause conjunctival hyperemia as measured by vasodilation. Compound was instilled and hyperemia was scored at 1, 2, 3, and 4 hours following dosing. Reported above is the cumulative incidence of hyperemia over the 4 hour period. Incidence of hyperemia (Bulbar Conjunctiva) was calculated as the percent of eyes scoring +2 or more, according to the following graded scale:

0 Normal appearance of vessels at limbus and rectus muscle

1 Enlargement of vessels normally visible at limbus and rectus muscle

2 Branching of vessels at limbus, additional vessels visible

3 Additional vessels visible in open bulbar conjunctival areas

4 Diffuse redness in open bulbar conjunctival areas

Monkey intraocular pressure (MIOP) were obtained from laser-induced hypertensive primates in the manner described in Examples 1 and 4 below at 1, 3, and 6 hours post-dose. 1-(5-isoquinolinesulfonyl)-2,5-dimethylpiperazine demonstrated a markedly superior IOP lowering effect.

EXAMPLE 1

The hydrochloride salt of Compound II, also known as fasudil hydrochloride or just fasudil, was topically administered to eyes of ocular normotensive and hypertensive monkeys, New Zealand Albino (NZA) and Dutch Belted (DB) rabbits. The results are presented in Table 1. As presented, Compound II effectively lowered IOP in both ocular normotensive and hypertensive (laser-induced) primates. In NZA rabbits, IOP was marketedly lowered below base line for the four hour dose response. Compound II also lowered IOP in the DB rabbit; however, the reduction in IOP was not sustained as in the NZA rabbit study.

TABLE 1 EFFECT OF FASUDIL ON IOP REDUCTION IN THE OCULAR HYPERTENSIVE AND NORMOTENSIVE MONKEY, NEW ZEALAND ALBINO AND DUTCH BELTED RABBIT ANIMAL Baseline PERCENT CHANGE FROM BASELINE MODEL IOP (mmHg) 1 HR 2 HR 3 HR 4 HR 6 HR Lasered MIOP 32.1 ± 3.2 21.9 ± 6.7 ↓ — 14.6 ± 6.5 ↓ — 23.4 ± 4.4 ↓ (n = 9)† Lasered MIOP 38.2 ± 3.3 15.9 ± 6.8 ↓ — 16.1 ± 4.8 ↓ —  7.1 ± 4.9 ↓ (n = 9) Normal MIOP 20.4 ± 1.4 18.9 ± 5.5 ↓ — 21.7 ± 5.2 ↓ — 11.1 ± 5.3 ↓ (n = 9) Dutch Belted 37.4 ± 0.6 33.7 ± 2.1 ↓ 18.0 ± 3.7 ↓ 10.8 ± 5.2 ↓  6.6 ± 3.9 ↓ — Rabbit (n = 7)†† Dutch Belted 32.1 ± 0.4 33.1 ± 2.7 ↓ 25.2 ± 3.5 ↓ 16.7 ± 3.9 ↓ 11.7 ± 4.0 ↓ — Rabbit (n = 7)†† NZA Rabbit 27.2 ± 0.3 36.2 ± 3.7 ↓ 35.5 ↓ 3.6 ↓ 26.1 ± 3.9 ↓ 22.5 ± 3.8 ↓ — (n = 7)†† All drugs were administered to eyes in a topical manner at a dose = 500 μg (2 × 25 μl). Fasudil was formulated in phosphate buffered saline containing 0.01% benzalkonium chloride. †No significant change in IOP from baseline values was observed in the contralateral untreated ocular normotensive eye or in a vehicle treated ocular hypertensive eye. ††No significant change in IOP from baseline values were observed in the contralateral untreated eye. MIOP = monkey intraocular pressure. n = number of animals in study.

EXAMPLE 2

Compound II (hydrochloride) was administered topically to the eyes of Dutch Belted (DB) rabbits in doses of 75 and 150 μg. The results are presented in Table 2.

TABLE 2 DOSE-RESPONSE STUDIES OF FASUDIL ON IOP IN THE DUTCH BELTED RABBIT Baseline Percent Change from Baseline Compound IOP (mmHg) 0.5 hr 1 hr 2 hr 3 hr 4 hr Group 1 33.0 ± 0.8 8.8 ± 3.8 ↓ 11.5 ± 3.2 ↓ 14.6 ± 3.5 ↓ 3.4 ± 2.7 ↓ 0.5 ± 3.2 ↑ Fasudil 150 μg OD Group 1 33.8 ± 0.6 3.6 ± 1.9 ↓  3.7 ± 2.4 ↓  5.7 ± 2.6 ↓   0 ± 2.4 ↓ 2.1 ± 3.2 ↑ Vehicle OS Group 2 34.3 ± 0.8 3.2 ± 2.8 ↓  3.3 ± 1.9 ↓  1.7 ± 2.7 ↓ 5.2 ± 2.2 ↓ 2.9 ± 2.1 ↓ Fasudil 75 μg OD Group 2 33.8 ± 0.6 1.1 ± 0.6 ↑  5.9 ± 2.6 ↑  6.0 ± 3.9 ↑ 4.5 ± 1.9 ↑ 1.9 ± 3.4 ↑ Vehicle OS All drugs were administered to eyes in a topical manner (1 × 30 μl). All compounds were formulated in a phosphate buttered saline containing 0.01% benzalkonium chloride. N = 6 animals/group; OD = drug treated eye; OS = vehicle treated contralateral eye.

EXAMPLE 3

A dose study similar to that described in Example 2 was conducted with the NZA rabbit. Compound II (hydrochloride) was administered in a topical ocular fashion in doses of 50, 125 and 250 μg. The results of this study are presented in Table 3.

TABLE 3 DOSE-RESPONSE STUDIES OF FASUDIL ON IOP IN THE NEW ZEALAND ALBINO RABBIT Baseline Percent Change from Baseline Compound IOP (mmHg) 0.5 hr 1 hr 2 hr 3 hr 4 hr Group 1 20.6 ± 0.3 5.5 ± 6.7 ↓ 21.1 ± 5.4 ↓ 24.9 ± 6.1 ↓ 25.1 ± 4.1 ↓ 16.3 ± 4.0 ↓ Fasudil 250 μg OD Group 2 21.2 ± .5  1.1 ± 3.7 ↓  4.4 ± 3.4 ↑  2.7 ± 3.2 ↑  2.7 ± 3.9 ↑  5.4 ± 3.6 ↑ Vehicle OS Group 2 20.4 ± .7  2.8 ± 3.8 ↑ 11.6 ± 2.9 ↓ 11.0 ± 4.7 ↓  7.0 ± 4.8 ↓  5.1 ± 2.7 ↓ Fasudil 125 μg OD Group 2 21.3 ± .6  5.3 ± 2.6 ↑  8.3 ± 6.0 ↑  7.3 ± 4.6 ↑  7.2 ± 5.3 ↑ 17.1 ± 6.5 ↑ Vehicle OS Group 3 21.3 ± .5  1.6 ± 3.0 ↓  3.2 ± 3.1 ↑  2.1 ± 4.7 ↑  1.7 ± 4.3 ↓ 10.8 ± 5.7 ↑ Fasudil 50 μg Group 3 21.4 ± .8  6.7 ± 4.1 ↑  9.1 ± 1.7 ↑  3.6 ± 3.3 ↑  9.8 ± 7.6 ↑  7.4 ± 4.5 ↑ Vehicle OS All drugs were administered to eyes in a topical manner (1 × 30 μl). All compounds were formulated in a phosphate buttered saline containing 0.01% benzalkonium chloride. N = 6 animals/group; OD = drug treated eye; OS = vehicle treated contralateral eye.

EXAMPLE 4

The effect of repeated doses of Compound II on the magnitude and duration of IOP reduction was evaluated in ocular normotensive monkeys. As shown in Table 4, a total of 900 μg of Compound II (hydrochloride) administered in three doses, ten minutes apart, resulted in significant IOP reduction.

TABLE 4 EFFECT OF REPEATED DOSES OF FASUDIL ON IOP IN THE OCULAR NORMOTENSIVE CYNOMOLGUS MONKEY Baseline IOP Percent Change from Baseline Compound (mmHg) 1 hr 3 hr 5 hr Fasudil 20.6 ± 0.8 23.1 ± 2.8 ↓ 23.1 ± 3.3 ↓ 19.3 ± 3.2 ↓ 900 μg OS Vehicle 20.2 ± 0.8 4.1 ± 1.8 ↓ 0.3 ± 4.4 ↑ 1.1 ± 3.7 ↓ 3 × 30 μl OS Fasudil was administered 3 × 30 μl topically (1 × 30 μl, 10 minutes apart). N = 10 for drug treated and N = 5 for vehicle. Fasudil was formulated in a phosphate buttered saline containing 0.01% benzalkonium chloride.

EXAMPLE 5

Topical Ophthalmic Formulation Ingredient % (w/v) Compound II (hydrochloride) 1.5  Benzalkonium chloride 0.01 Phosphate buffered saline q.s. to 100

EXAMPLE 6

Topical Ophthalmic Formulation With Sustained Release Ingredient % (w/v) Compound II (hydrochloride) 1.0 Carbomer 934P or Carbomer 974P 0.5 NaCl 0.4 Mannitol 2.4 Disodium edetate 0.01 BAC 0.01 Water for Injection q.s. to 100 NaOH or HCl to adjust pH q.s.

EXAMPLE 7

Systemic Formulation (Oral) Ingredient Weight Proportion Compound II (hydrochloride) 50 Sodium Citrate 20 Alginic Acid 5 Polyvinylpyrrolidone 15 Magnesium Stearate 5

Preparation: The dry composition is thoroughly blended, tablets are punched from the resulting mixture, each tablet being of such size that it contains 10 mg of Compound II (hydrochloride).

EXAMPLE 8

Intraocular or Periocular Formulation (For Intravitreal for Periocular Injection) Ingredient % (w/v) Compound II (hydrochloride) 0.002 Sterile balanced salt solution q.s. to 100

EXAMPLE 9 Method of Treatment (Topical)

A patient suffering from elevated IOP and/or visual field loss is treated by the topical administration of the formulation of Example 5. One 30 μl drop of the formulation is administered one to four times per day to the affected eye(s) thereby reducing the IOP and/or the progression of visual field loss.

EXAMPLE 10 Method of Treatment (Systemic)

A patient suffering from elevated IOP and/or visual field loss is treated by the oral administration of the formulation of Example 7. One or more tablets of the formulation are administered orally 1 to 4 times per day thereby reducing the IOP and/or the progression of visual field loss.

EXAMPLE 11 Method of Treatment (Intraocular or Periocular)

A patient suffering from elevated IOP and/or visual field loss is treated by the intravitreal or periocular administration of the formulation of Example 8. Ten to twenty-five microliters of the formulation are administered 1 time per month to the affected eye(s) thereby reducing the IOP and/or the progression of visual field loss.

Using the excipients of and/or following the procedures of the foregoing Examples 5-11, compositions and treatments are employed substituting an equivalent concentration/amount of a compound of formula (IA), and in particular 1-(5-isoquinolinesulfonyl)-2,5-dimethylpiperazine, for Compound II (hydrochloride) disclosed in such Examples. Similar or superior results are obtained.

EXAMPLE 12

Other isoquinolinesulfonamides were topically administered to the eyes of New Zealand Albino (NZA) rabbits. The results are presented in Table 5 below.

TABLE 5 Effect of other isoquinolinesulfonylamides on IOP in the NZA Rabbit Baseline IOP Percent Change from Baseline Compound (mmHg) 1 hr 3 hr 5 hr

20.4 ± 0.8 14.6 ± 2.6 ↓  7.2 ± 4.1 ↓  0.9 ± 3.5 ↑

19.5 ± 0.5  7.7 ± 4.3 ↓ 14.5 ± 0.5 ↓  0.8 ± 2.3 ↓

15.6 ± 0.5 16.8 ± 5.7 ↑ 16.0 ± 5.7 ↑ 37.0 ± 4.1 ↑

16.2 ± 0.3  9.9 ± 3.5 ↓  9.4 ± 1.9 ↓  3.3 ± 3.8 ↑

All drugs were administered to eyes in a topical manner at a dose=500 μg (2×25 μl). All compounds were formulated in phosphate buffered saline containing 0.01% benzalkonium chloride, and in all instances N=7.

The invention has been described by reference to certain preferred embodiments; however, it should be understood that it may be embodied in other specific forms or variations thereof without departing from its spirit or essential characteristics. The embodiments described above are therefore considered to be illustrative in all respects and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description. 

What is claimed is:
 1. A method of treating glaucoma, ocular hypertension, ocular ischemia and related disorders in a patient with one or more of such conditions, comprising administering to said patient a composition comprising an ophthalmically effective amount of a compound of formula (IA):

wherein: R¹=H, OH, or Cl; A=an ethylene group, unsubstituted or substituted with an alkyl group having 1 to 6 carbons; R⁴=H or an alkyl group having 1 to 3 carbons; R⁵=an alkyl group having 1 to 3 carbons; and R⁶=H or an alkyl group having 1 to 6 carbons; together with pharmaceutically acceptable salts thereof; with the proviso that the following compounds are excluded:

 and pharmaceutically acceptable salts thereof.
 2. The method of claim 1, wherein the administration of the composition is effected topically.
 3. The method of claim 2, wherein the final composition concentration of the compound of formula (IA) is between about 0.001 and about 10.0 wt %.
 4. The method of claim 3, wherein the final composition concentration of the compound of formula (IA) is between about 0.01 and about 3.0 wt %.
 5. The method of claim 4, wherein the final composition concentration of the compound of formula (IA) is between about 0.1 and about 2.0 wt %.
 6. The method of claim 2, wherein the composition further comprises a sustained release component.
 7. The method of claim 6, wherein the sustained release component is selected from the group consisting of: mucomimetic polymers, gelling polysaccharides, finely-divided drug carrier substrates, and combinations thereof.
 8. The method of claim 2, wherein for the compound of formula (IA): R¹=H, OH, or Cl; A=an ethylene group unsubstituted or substituted with an alkyl group having 1 to 3 carbons; R⁴=H or an alkyl group having 1 to 3 carbon; R⁵=an alkyl group having 1 to 3 carbons; and R⁶=H or an alkyl group having 1 to 6 carbons.
 9. The method of claim 8, wherein for the compound of formula (IA): R¹=H, OH, or Cl; A=an ethylene group unsubstituted or substituted with an alkyl group having 1 to 3 carbons; R⁴=H; R⁵=an alkyl group having 1 carbon; and R⁶=H or an alkyl group having 1 to 3 carbons.
 10. The method of claim 9, wherein for the compound of formula (IA): R¹, R⁴ and R⁶=H; and A=an ethylene group substituted with an alkyl group having 1 carbon.
 11. A method of treating glaucoma or ocular hypertension in a mammal, comprising topically administering to the affected eye of the mammal an intraocular pressure lowering effective amount of 1-(5-isoquinolinesulfonyl)-2,5-dimethylpiperazine. 